1. ^*From the Division of Neuropathology, Alzheimer's Disease Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, U.S.A.
2. ^‡Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, U.S.A.
3. ^†MGH Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, U.S.A.

Correspondence: Suzanne M de la Monte, MGH Cancer Center, Room 7308, MGH East, 149 13th Street, Charlestown, MA 02129 U.S.A.

Received 7 February 1996; Revised 30 January 1997; Accepted 30 January 1997.

Abstract

Neuronal thread proteins (NTP) are a family of phosphoproteins expressed during neuritic sprouting. The 15 to 18 kD NTP cluster is associated with development and neuronal differentiation, whereas the 21 kD and 39 to 42 kD species are overexpressed in Alzheimer's disease, correlating with neurodegenerative sprouting and synaptic disconnection. Empirical observations suggested that NTP might also be modulated with central nervous system injury and stroke. In this study of both human and experimental (rat) focal cerebral infarcts, in situ hybridization and immunocytochemical staining revealed NTP gene expression up-regulated in perifocal neurons. These findings were confirmed by quantitative Northern and Western blot analyses. Moreover, Western blot analysis demonstrated selectively increased expression of the 15 to 18 kD NTP species during the acute, subacute, and healing phases of cerebral infarction in both humans and experimental animals, corresponding with the expected period of neuronal repair. These results suggest an additional role for the 15 to 18 kD NTP species in neuritic sprouting required for neuronal regeneration after injury in the mature central nervous system.